Variant #0000862591 (NC_000011.9:g.58891964del, NM_198947.3:c.394del (FAM111B))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.58891964del
DNA change (hg38) -
Published as FAM111B(NM_198947.3):c.394delT (p.Y132Mfs*6), FAM111B(NM_198947.4):c.394del (p.(Tyr132Metfs*6))
ISCN -
DB-ID FAM111B_000015 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM111B NM_198947.3 -/. - c.394del r.(?) p.(Tyr132Metfs*6)


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